| Weight | 181.191 g/mol |
|---|---|
| Formula | C9H11NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
L-tyrosine
Tyrosine · L Tyrosine · para Tyrosine
25619-78-7, 60-18-4, 556-02-5
Score:
#239 in Biochemistry
,
#921 in Biology
,
#1016 in Chemistry
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- Sigma-Aldrich - L-tyrosine20.50 - 870.30 USD
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- TCI - L-tyrosine24.00 - 199.00 USD
- Signal transduction by receptors with tyrosine kinase activity (Cell, 1990)
- Cell Signaling by Receptor Tyrosine Kinases (Cell, 2000)
- Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia (The New England Journal of Medicine, 2001)
- Specificity of receptor tyrosine kinase signaling: Transient versus sustained extracellular signal-regulated kinase activation (Cell, 1995)
- PTEN, a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate Cancer (Science, 1997)
- Genistein, a specific inhibitor of tyrosine-specific protein kinases. (Journal of Biological Chemistry, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tyrosine
- L Tyrosine
- para Tyrosine
- Tyrosine, L-isomer
- para-Tyrosine
- Tyrosine, L isomer
-
SMILESC1=CC(=CC=C1CC(C(=O)O)N)O
-
InChIKeyOUYCCCASQSFEME-UHFFFAOYSA-N
- Pubchem - L-tyrosine
- Wikipedia - tyrosine
Tyrosine (Tyr or Y) or 4-hydroxyphenylalanine is one of the 20 standard amino acids that are used by cells to synthesize proteins. It is a non-essential amino acid with a polar side group. Its codons are UAC and UAU.
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L-tyrosine
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